A General and Efficient Synthesis of Substituted Mono-and Di-indole C-nucleoside Analogs by Sequenti

来源 :2014年全国糖生物学学术会议 | 被引量 : 0次 | 上传用户:engcourse
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The synthesis of substituted mono-and di-indole C-nucleoside analogs has been achieved by the NaAuCl4 catalyzed sequential Sonogashira coupling/heteroannulation reactions of substituted 2-Iodoanilines with various sugar terminal alkynes in one pot.
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